Toward the Integration of a Silicon/Graphite Anode-Based Lithium-Ion Battery in Photovoltaic Charging Battery Systems.

Solar photovoltaic (PV) energy generation is highly dependent on weather conditions and only applicable when the sun is shining during the daytime, leading to a mismatch between demand and supply. Merging PVs with battery storage is the straightforward route to counteract the intermittent nature of solar generation. Capacity (or energy density), overall efficiency, and stability at elevated temperatures are among key battery performance metrics for an integrated PV-battery system. The performance of high-capacity silicon (Si)/graphite (Gr) anode and LiNi0.6Mn0.2Co0.2O2 (NMC622) cathode cells at room temperature, 45, and 60 °C working temperatures for PV modules are explored. The electrochemical performance of both half and full cells are tested using a specially formulated electrolyte, 1 M LiPF6 in ethylene carbonate: diethyl carbonate, with 5 wt % fluoroethylene carbonate, 2 wt % vinylene carbonate, and 1 wt % (2-cyanoethyl)triethoxysilane. To demonstrate solar charging, perovskite solar cells (PSCs) are coupled to the developed batteries, following the evaluation of each device. An overall efficiency of 8.74% under standard PV test conditions is obtained for the PSC charged lithium-ion battery via the direct-current-direct-current converter, showing the promising applicability of silicon/graphite-based anodes in the PV-battery integrated system.

Long-Term Stability of Redox Mediators in Carbonate Solvents.

Scanning electrochemical microscopy (SECM) used in the feedback mode is one of the most powerful versatile analytical tools used in the field of battery research. However, the application of SECM in the field of lithium-ion batteries (LIBs) faces challenges associated with the selection of a suitable redox mediator due to its high reactivity at low potentials at lithium metal or lithiated graphite electrodes. In this regard, the electrochemical/chemical stability of 2,5-di-tert-butyl-1,4-dimethoxybenzene (DBDMB) is evaluated and benchmarked with ferrocene. This investigation is systematically carried out in both linear and cyclic carbonates of the electrolyte recipe. Measurements of the bulk current with a microelectrode prove that while DBDMB decomposes in ethyl methyl carbonate (EMC)-containing electrolyte, bulk current remains stable in cyclic carbonates, ethylene carbonate (EC) and propylene carbonate (PC). Ferrocene was studied as an alternative redox mediator, showing superior electrochemical performance in ethyl methyl carbonate-containing electrolytes in terms of degradation. The resulting robustness of ferrocene with SECM is essential for a quantitative analysis of battery materials over extended periods. SECM approach curves depict practical problems when using the decomposing DBDMB for data acquisition and interpretation. This study sheds light towards the use of SECM as a probing tool enabled by redox mediators.

Production of high-energy Li-ion batteries comprising silicon-containing anodes and insertion-type cathodes.

Rechargeable Li-based battery technologies utilising silicon, silicon-based, and Si-derivative anodes coupled with high-capacity/high-voltage insertion-type cathodes have reaped significant interest from both academic and industrial sectors. This stems from their practically achievable energy density, offering a new avenue towards the mass-market adoption of electric vehicles and renewable energy sources. Nevertheless, such high-energy systems are limited by their complex chemistry and intrinsic drawbacks. From this perspective, we present the progress, current status, prevailing challenges and mitigating strategies of Li-based battery systems comprising silicon-containing anodes and insertion-type cathodes. This is accompanied by an assessment of their potential to meet the targets for evolving volume- and weight-sensitive applications such as electro-mobility.

A Review on Li+ /H+ Exchange in Garnet Solid Electrolytes: From Instability against Humidity to Sustainable Processing in Water.

Garnet-based Li-ion conductors are one of the most promising oxide-ceramic solid electrolytes for next-generation Li batteries. However, they undergo a Li+ /H+ exchange (LHX) reaction with most protic solvents used in component manufacturing routes and even with moisture in ambient air. These protonated garnets show a lower Li-ionic conductivity, and even if only the surface is protonated, this degraded layer hinders the Li-ion exchange with, for example, a metallic Li anode. Furthermore, the resulting unstable surface properties during the processing in air lead to challenges with respect to reproducibility of the final component performance, limiting their commercial applicability. However, in recent years, the knowledge about the underlying chemical mechanisms has led to the development of mitigation strategies and enabled a push of this promising material class towards sustainable and scalable fabrication routes. This Minireview covers the following four aspects, which are relevant for a comprehensive understanding of these developments: (1) reports of LHX phenomenon in garnets exposed to air and solvents; (2) recent understandings of the fundamentals and properties of LHX; (3) strategies to prevent LHX and to recover garnets; and (4) sustainable application of LHX for material processing and energy-related devices.

Confronting the Challenges of Next-Generation Silicon Anode-Based Lithium-Ion Batteries: Role of Designer Electrolyte Additives and Polymeric Binders.

Silicon has emerged as the next-generation anode material for high-capacity lithium-ion batteries (LIBs). It is currently of scientific and practical interest to encounter increasingly growing demands for high energy/power density electrochemical energy-storage devices for use in electric vehicles (xEVs), renewable energy sources, and smart grid/utility applications. Improvements to existing conventional LIBs are required to provide higher energy, longer cycle lives. This is attributed to its unparalleled theoretical capacity (4200 mAh g-1 for Li4.4 Si), which is approximately 10 times higher than that of a state-of-the-art graphitic anode (372 mAh g-1 for LiC6 ), with a suitable operating voltage, natural abundance, environmental benignity, nontoxicity, high safety, and so forth. However, despite the overwhelming beneficial features, the practical integration of LIBs containing a silicon anode beyond the commercial niche is hampered by unavoidable challenges, such as excessive volume changes during the (de-)alloying process, inherently low electrical and ionic conductivities, an unstable solid-electrolyte interphase, and electrolyte drying out. Among various extenuating strategies, non-electrode factors encompassing electrolyte additives and polymeric binders are regarded as the most economical, and effective approaches towards circumventing these disadvantages are in short supply. With the aim of providing an in-depth insight into rapidly growing accounts of electrolyte additives and binders for use with silicon anode-based LIBs, this Review assesses the current state of the art of research and thereby examines opportunities to open up new avenues for the practical realization of these silicon anode-based LIBs.

Utilization of a right-handed coiled-coil protein from archaebacterium Staphylothermus marinus as a carrier for cisplatin.

BACKGROUND: The nano-sized right-handed coiled-coil (RHCC) protein, originating from the archaebacterium Staphylothermus marinus, is stable at high salt concentrations, high temperatures, high pressures and extremes of pH. Its crystal structure reveals four hydrophobic cavities which can incorporate heavy metals. Nano-sized compounds have been used to carry cytotoxic drugs to tumours, avoiding delivery to healthy tissue, in part due to enhanced permeability in tumour blood vessels (enhanced permeability and retention effect). MATERIALS AND METHODS: The ability of RHCC to carry the platinum-containing chemotherapeutic drug cisplatin to cells, while retaining the cytotoxic potential was tested both in vitro and in vivo. RESULTS: RHCC was able to bind and enter cells in vitro and was not severely toxic or immunogenic in mice. Moreover, RHCC incorporated cisplatin, without inhibiting the cytotoxic potential of the drug against tumour cell lines in vitro or in vivo. CONCLUSION: RHCC can be used as a carrier of cisplatin without abrogating the effect of the drug.

Robust self-assembled monolayers of Ru(II) and Os(II) polypyridines on gold surfaces: exploring new potentials.

Metal complexes [M(phtpy)(pztpy)](PF(6))(2) (phtpy = 4'-phenyl-2,2':6',2''-terpyridine, pztpy = 4'-(N-piperazinyl)-2,2':6',2''-terpyridine, M = Ru, Os) were prepared and examined spectroscopically and electrochemically. The piperazine attachment was found to significantly modify the photophysical and electrochemical properties compared to the parent bis-terpyridine complexes, causing a red-shift of the (1)MLCT (23 nm, 53.9 eV) and a substantial cathodic shift of the redox potential (0.3 V for Ru, 0.23 V for Os). Self-assembled monolayers (SAMs) of the complexes on polished gold electrodes were generated simply by the in situ formation of a dithiocarbamate (DTC) anchoring group at the terminal piperazinyl nitrogen on the pztpy ligand. Cyclic voltammetry revealed that the monolayers show excellent reversible behaviour and exceptional stability. The high stability of the SAMs is attributed to the strong bidentate attachment to the gold surface of the DTC tether and the favourable low oxidation potentials of the complexes which result from the electron-rich piperazine nitrogen on the pztpy ligand. Such DTC-based SAMs demonstrate a substantial improvement over commonly-employed thiol-based systems, and offer new scope for future development.

Wiring terpyridine: approaches to alkynylthienyl 2,2':6',2''-terpyridines.

The reaction of triisopropylsilylethyne or trimethylsilylethyne with 4'-(5-bromo-2-thienyl)-2,2':6',2''-terpyridine () leads to 4'-(5-triisopropylsilylethynyl-2-thienyl)-2,2':6',2''-terpyridine () or 4'-(5-trimethylsilylethynyl-2-thienyl)-2,2':6',2''-terpyridine (). The latter compound may be deprotected to give 4'-(5-ethynyl-2-thienyl)-2,2':6',2''-terpyridine (). Treatment of the complexes [Ru()(2)][PF(6)](2), [Ru(tpy)()][PF(6)](2) and [Ru()(2)][PF(6)](2) ( = 4'-(4-bromo-2-thienyl)-2,2':6',2''-terpyridine) with triisopropylsilylethyne yields the corresponding homoleptic and heteroleptic alkynylthienyl-terminated ruthenium(ii) complexes, for which spectroscopic and electrochemical data are presented. The reaction of [RuCl(2)(DMSO)(4)] with leads to [Ru()(2)][PF(6)](2), in which the tpy ligands bear conjugated thienyl and alkynyl groups; the latter can also be accessed by deprotection of [Ru()(2)][PF(6)](2). The single-crystal structures of ligands and , and of [Ru()(tpy)][BPh(4)](2).1.3MeCN, [Ru()(2)][PF(6)](2).2MeNO(2), 2{[Ru()(2)][PF(6)](2)}.5MeCN, [Ru()(2)][PF(6)](2) and [Ru()(2)][PF(6)](2).MeCN are presented, and among the homoleptic complexes, pi-stacking interactions between thiophene and pyridine rings leading to pairs of associated cations provide a common structural motif.

Scanning electrochemical microscopy under illumination: an elegant tool to directly determine the mobility of charge carriers within dye-sensitized nanostructured semiconductors.

The diffusion constant of the ferrocenium ion in dye-sensitized nanostructured materials has been determined by time-of-flight experiments under working solar cell conditions with scanning electrochemical microscopy.

DFT-INDO/S modeling of new high molar extinction coefficient charge-transfer sensitizers for solar cell applications.

A new ruthenium(II) complex, tetrabutylammonium [ruthenium (4-carboxylic acid-4'-carboxylate-2,2'-bipyridine)(4,4'-di(2-(3,6-dimethoxyphenyl)ethenyl)-2,2'-bipyridine)(NCS)(2)] (N945H), was synthesized and characterized by analytical, spectroscopic, and electrochemical techniques. The absorption spectrum of the N945H sensitizer is dominated by metal-to-ligand charge-transfer (MLCT) transitions in the visible region, with the lowest allowed MLCT bands appearing at 25 380 and 18 180 cm(-1). The molar extinction coefficients of these bands are 34 500 and 18 900 M(-1) cm(-1), respectively, and are significantly higher when compared to than those of the standard sensitizer cis-dithiocyanatobis(4,4'-dicarboxylic acid-2,2'-bipyridine)ruthenium(II). An INDO/S and density functional theory study of the electronic and optical properties of N945H and of N945 adsorbed on TiO(2) was performed. The calculations point out that the top three frontier-filled orbitals have essentially ruthenium 4d (t(2g) in the octahedral group) character with sizable contribution coming from the NCS ligand orbitals. Most critically the calculations reveal that, in the TiO(2)-bound N945 sensitizer, excitation directs charge into the carboxylbipyridine ligand bound to the TiO(2) surface. The photovoltaic data of the N945 sensitizer using an electrolyte containing 0.60 M butylmethylimidazolium iodide, 0.03 M I(2), 0.10 M guanidinium thiocyanate, and 0.50 M tert-butylpyridine in a mixture of acetonitrile and valeronitrile (volume ratio = 85:15) exhibited a short-circuit photocurrent density of 16.50 +/- 0.2 mA cm(-2), an open-circuit voltage of 790 +/- 30 mV, and a fill factor of 0.72 +/- 0.03, corresponding to an overall conversion efficiency of 9.6% under standard AM (air mass) 1.5 sunlight, and demonstrated a stable performance under light and heat soaking at 80 degrees C.

Favourable mediation of crystal contacts by cocoamidopropylbetaine (CAPB).

Crystals of excellent quality are a prerequisite for high-resolution X-ray data. However, in refinement protocols of crystallization conditions it is often difficult to obtain the right combination of, for example, protein concentration, drop size, temperature and additives. A novel approach for optimizing crystal contacts in a most favourable fashion by performing crystallization setups with the zwitterionic surfactant cocoamidoproylbetaine (CAPB) is introduced. In the presence of this surfactant, highly diffracting crystals were obtained. Here, data from a right-handed coiled coil (RHCC) in complex with CAPB at 1.4 A resolution are presented. The addition of CAPB using otherwise identical crystallization conditions and the same X-ray source caused an improvement in resolution from 2.9 to 1.4 A.

Hairpin helicates: a missing link between double-helicates and trefoil knots.

We have prepared a novel ligand in which two qpy metal-binding domains are linked by a polyoxyethylene spacer. The new ligand reacts with copper(ii) salts to form dinuclear double helicates with a hairpin structure. The hairpin complex and a model complex have been structurally characterised. The hairpin structure is formed regioselectively as the head-to-tail (HT) stereoisomer. Detailed electrochemical and spectroelectrochemical studies of the complexes are reported.

Self-assembled monolayers of Ru/Os dinuclear complexes: probing monolayer structure and interaction energies by electrochemical means.

Monolayers of [Ru(bpy)2(micro-1)M2][PF6]4 salts (M = Os, Ru; bpy = 2,2'-bipyridine, 1 = 4'-(2,2'-bipyridin-4-yl)-2,2':6',2' '-terpyridine, tpy = 2,2':6',2' '-terpyridine, and 2 = 4'-(4-pyridyl)-2,2':6',2' '-terpyridine) were self-assembled on platinum and investigated by fast-scan electrochemistry. The electrochemistry of the complexes in solution and confined to the surface in self-assembled monolayers (SAMs) exhibited an almost ideal behavior. Scan-rate-dependent measurements of the peak current density (jp) were used to determine interaction energies within the monolayer. It is shown that the tpy coordination sites of the dinuclear complexes interact more strongly within the SAM than the bipyridine-coordinated fragments. This result was supported by peak potential shifts, which are due to interaction forces in SAMs. The alignment of the rodlike complexes relative to the surface is discussed, and the results of molecular mechanics calculations indicate that the species adopt a tilted orientation.

Electrochemical probing of ground state electronic interactions in polynuclear complexes of a new heteroditopic ligand.

The synthesis and electronic properties of dinuclear ([(bipy)2Ru(I)M(terpy)][PF6]4(bipy = 2,2'-bipyridine, terpy = 2,2':6',2''-terpyridine; M = Ru, Os)) and trinuclear ([[(bipy)2Ru(I)]2M][PF6]6 M = Ru, Os, Fe, Co) complexes bridged by 4'-(2,2'-bipyridin-4-yl)-2,2':6',2''-terpyridine (I) have been investigated and are compared with those of mononuclear model complexes. The electrochemical analysis using cyclic voltammetry and differential pulse voltammetry reveals that there are no interactions in the ground state between adjacent metal centres. However, there is strong electronic communication between the 2,2'-bipyridine and 2,2':6',2''-terpyridine components of the bridging ligand. This conclusion is supported by a step-by-step reduction of the dinuclear and trinuclear complexes and the assignment of each electrochemical process to localised ligand sites within the didentate and terdentate domains. The investigation of the electronic absorption and emission spectra reveals an energy transfer in the excited state from the terminating bipy-bound metal centres to the central terpy-bound metal centre. This indicates that the bridge is able to facilitate energy transfer in the excited state between the metal centres despite the lack of interactions in the ground state.

Redox and spectroscopic orbitals in Ru(II) and Os(II) phenolate complexes.

A detailed spectroscopic and electrochemical study of a series of novel phenolate bound complexes, of general formulas [M(L-L)(2)(box)](PF(6)), where M is Os and Ru, L-L is 2,2-bipyridine or 2,2-biquinoline, and box is 2-(2-hydroxyphenyl)benzoxazole, is presented. The objectives of this study were to probe the origin of the LUMOs and HOMOs in these complexes, to elucidate the impact of metal and counter ligand on the electronic properties of the complex, and to identify the extent of orbital mixing in comparison with considerably more frequently studied quinoid complexes. [M(L-L)(2)(box)](PF(6)) complexes exhibit a rich electronic spectroscopy extending into the near infrared region and good photostability, making them potentially useful as solar sensitizers. Electrochemistry and spectroscopy indicate that the first oxidation is metal based and is associated with the M(II)/(III) redox states. A second oxidative wave, which is irreversible at slow scan rates, is associated with the phenolate ligand. The stabilities of the oxidized complexes are assessed using dynamic electrochemistry and discussed from the perspective of metal and counter ligand (LL) identity and follow the order of increasing stability [Ru(biq)(2)(box)](+) < [Ru(bpy)(2)(box)](+) < [Os(bpy)(2)(box)](+). Electronic and resonance Raman spectroscopy indicate that the lowest energy optical transition for the ruthenium complexes is a phenolate (pi) to L-L (pi) interligand charge-transfer transition (ILCT) suggesting the HOMO is phenolate based whereas electrochemical data suggest that the HOMO is metal based. This unusual lack of correlation between redox and spectroscopically assigned orbitals is discussed in terms of metal-ligand orbital mixing which appears to be most significant in the biquinoline based complex.

A rod-like polymer containing (Ru(terpy)2) units prepared by electrochemical coupling of pendant thienyl moieties.

A new rod-like coordination polymer consisting of (Ru-(terpy)2) motifs bridged by bithiophene units has been prepared by electrochemical polymerisation in acidic organic medium.

Electronic energy transfer and collection in luminescent molecular rods containing ruthenium(II) and osmium(II) 2,2':6',2"-terpyridine complexes linked by thiophene-2,5-diyl spacers.

The electronic absorption spectra, luminescence spectra and lifetimes (in MeCN at room temperature and in frozen n-C3H7CN at 77 K), and electrochemical potentials (in MeCN) of the novel dinuclear [(tpy)Ru(3)Os(tpy)]4+ and trinuclear [(tpy)Ru(3)Os(3)Ru(tpy)]6- complexes (3 = 2,5-bis(2,2':6',2''-terpyridin-4-yl)thiophene) have been obtained and are compared with those of model mononuclear complexes and homometallic [(tpy)Ru(3)Ru(tpy)]4+, [(tpy)Os(3)Os(tpy)]4+ and [(tpy)Ru(3)Ru(3)Ru(tpy)]6+ Complexes. The bridging ligand 3 is nearly planar in the complexes, as seen from a preliminary X-ray determination of [(tpy)Ru(3)Ru(tpy)][PF6]4, and confers a high degree of rigidity upon the polynuclear species. The trinuclear species are rod-shaped with a distance of about 3 nm between the terminal metal centres. For the polynuclear complexes, the spectroscopic and electrochemical data are in accord with a significant intermetal interaction. All of the complexes are luminescent (phi in the range 10(-4)-10(-2) and tau in the range 6-340 ns, at room temperature), and ruthenium- or osmium-based luminescence properties can be identified. Due to the excited state properties of the various components and to the geometric and electronic properties of the bridge, Ru --> Os directional transfer of excitation energy takes place in the complexes [(tpy)Ru(3)Os(tpy)]4+ (end-to-end) and [(tpy)Ru(3)Os(3)Ru(tpy)]6+ (periphery-to-centre). With respect to the homometallic case, for [(tpy)Ru(3)Os(3)Ru(tpy)]6+ excitation trapping at the central position is accompanied by a fivefold enhancement of luminescence intensity.